43 results · 22ms · Sources: EU EUDAMED, US FDA

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FIXPINE II SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

Oticon

FDA UDI
Oticon A/S·05707131167453·ACTO, ITC P R BE

Osstell SmartPeg Type 100

FDA UDI
Osstell AB·09010522002117·ISQ Measurement Peg

CONKLUSION

FDA UDI
SIGNUS Medizintechnik GmbH·04047844013700·The CONKLUSION Pedicle Screw System is a spinal...

Ear Tip PM007 Pack/100 pcs. (Grason)

FDA UDI
PATH medical GmbH·04260223142062·PATH MEDICAL is not manufacturer or Labeler of ...

Disposable Sterile Kit

FDA UDI
RESTORATION ROBOTICS, INC.·00850470007098·

Indus®

FDA UDI
SPINEFRONTIER, INC.·00190361001447·Invue Max, Four Level ACP, 65mm

Zavation

FDA UDI
Zavation LLC·00197157002046·6.5mm Tap

UA Transfer Die

FDA UDI
BICON, LLC·00813110026897·UA6 SP-TP Transfer Dies (2)

N/A

FDA UDI
Doppkon GmbH & Co. KG·04262494464034·Grasping Forceps Straight Jaw D 5.0mm, WL 150mm

Ear Tip PM007H Pack/100 pcs.

FDA UDI
PATH medical GmbH·04260223146862·7 mm mushroom ear tip, hard version

DIAMOND ANTERIOR CERVICAL PLATE SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

COULTER HMX ANALYZER, MODEL 6605523, COULTER HMX WITH AUTOLOADER, MODEL 6605526

FDA 510(k)
FDA Class 2 ·Hematology

LINEAR? ST

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·July 30, 2025

UNKNOWN IV CATHETER

FDA Adverse Event
Injury ·BD (SUZHOU)·Product code FOZ·January 13, 2016

LIFEPAK(R) 20E DEFIBRILLATOR/MONITOR

FDA Adverse Event
Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·May 8, 2013

ALLEGRETTO WAVE EYE-Q

FDA Adverse Event
Injury ·WAVELIGHT GMBH·Product code LZS·September 12, 2014

FIXODENT ADHESIVE CREAM (CALCIUM ZINC GANTREZ SALT 44.4%, CELLULOSE GUM 20%) CRE

FDA Adverse Event
Injury ·PROCTER & GAMBLE MFG. GMBH·Product code KOO·May 19, 2011

COULTER ISOTON III DILUENT

FDA Adverse Event
Malfunction ·BECKMAN COULTER·Product code GIF·May 1, 2014

COULTER ISOTON III DILUENT

FDA Adverse Event
Malfunction ·BECKMAN COULTER·Product code GIF·April 28, 2014